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A proteomic network approach across the ALS-FTD disease spectrum resolves clinical phenotypes and genetic vulnerability in human brain

Authors:Mfon E Umoh, Emory University School of MedicineEric Dammer, Emory UniversityJingting Dai, Emory University School of MedicineDuc M Duong, Emory University School of MedicineJames Lah, Emory UniversityAllan Levey, Emory UniversityMarla Gearing, Emory UniversityJonathan Glass, Emory UniversityNicholas Seyfried, Emory University

Date:2017

Publisher:Wiley Open Access

Publication Version:Final Published Version

License:Creative Commons Attribution 4.0 International

Inflammatory monocytes promote progression of Duchenne muscular dystrophy and can be therapeutically targeted via CCR2

Authors:Kamalika Mojumdar, McGill UniversityFeng Liang, McGill UniversityChristian Giordano, McGill UniversityChristian Lemaire, McGill UniversityGawiyou Danialou, McGill UniversityTatsuma Okazaki, McGill UniversityJohanne Bourdon, McGill UniversityMoutih Rafei, University of MontrealJacques Galipeau, Emory UniversityMaziar Divangahi, McGill UniversityBasil J. Petrof, McGill University

Date:2014

Publisher:Wiley Open Access

Publication Version:Final Published Version

License:Creative Commons Attribution 4.0 International

Virally mediated Kcnq1 gene replacement therapy in the immature scala media restores hearing in a mouse model of human Jervell and Lange-Nielsen deafness syndrome

Authors:Qing Chang, Emory UniversityJianjun Wang, Emory UniversityQi Li, Emory UniversityYeunjung Kim, Emory UniversityBinfei Zhou, Emory UniversityYunfeng Wang, Fudan UniversityHuawei Li, Fudan UniversityXi Lin, Emory University

Date:2015

Publisher:Wiley Open Access

Publication Version:Final Published Version

License:Creative Commons Attribution 4.0 International

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A proteomic network approach across the ALS-FTD disease spectrum resolves clinical phenotypes and genetic vulnerability in human brain

Inflammatory monocytes promote progression of Duchenne muscular dystrophy and can be therapeutically targeted via CCR2

Virally mediated Kcnq1 gene replacement therapy in the immature scala media restores hearing in a mouse model of human Jervell and Lange-Nielsen deafness syndrome

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